김영독 교수
Young Dok Kim
성균관대학교 화학과 · 재료과학
연구실 소개
김영독 교수의 연구실은 나노구조 소재의 합성과 응용에 중점을 두며, 특히 메쉬형 금속 유기 프레임워크(MOF) 및 유기 네트워크 복합체, 나노입자 기반 촉매, 초친수성 표면 소재, 유기 태양전지 등에서의 응용을 연구하고 있습니다. 고도화된 표면 기능화와 나노구조 제어를 통해 에너지 및 환경 분야의 핵심 기술을 개발하고 있으며, 특히 수소 생산, 오염물질 제거, 센서 민감도 향상 등 실용적 응용에 기여하고자 합니다. 다양한 분석 기법과 이론 계산을 융합한 다학제적 접근이 특징입니다.
연구 현황
연구 성과 추이
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주요 논문
15This work reports the synthesis and application of metal-organic framework (MOF)@microporous organic network (MON) hybrid materials. Coating a MOF, UiO-66-NH2, with MONs forms hybrid microporous materials with hydrophobic surfaces. The original UiO-66-NH2 shows good wettability in water. In comparison, the MOF@MON hybrid materials float on water and show excellent performance for adsorption of a model organic compound, toluene, in water. Chemical etching of the MOF results in the formation of ho
Au nanoparticles grown on mildly sputtered Highly Ordered Pyrolytic Graphite (HOPG) surfaces were studied using Scanning Tunneling Microscopy (STM) and X-ray Photoelectron Spectroscopy (XPS). The results were compared with those of Ag nanoparticles on the same substrate. By varying the defect densities of HOPG and the Au coverages, one can create Au nanoparticles in various sizes. At high Au coverages, the structures of the Au films significantly deviate from the ideal truncated octahedral form:
Experimental and theoretical evidence is presented for the nondissociative chemisorption of O2 on free Au cluster anions (Aun-, n=number of atoms) with n=2, 4, 6 at room temperature, indicating that the stabilization of the activated di-oxygen species is the key for the unusual catalytic activities of Au-based catalysts. In contrast to Aun- with n=2, 4, 6, O2 adsorbs atomically on Au monomer anions. For the Au monomer neutral, calculations based on density functional theory reveal that oxygen sh
Mesoporous silica with mean pore size of ∼14 nm was coated by polydimethylsiloxane (PDMS) using a thermal deposition method. We showed that the inner walls of pores larger than ∼8 nm can be coated by thin layers of PDMS, and the surfaces consisting of PDMS-coated silica were superhydrophobic, with water contact angles close to 170°. We used the PDMS-coated silica as adsorbents of various gas-phase chemical warfare agent (CWA) simulants. PDMS-coated silica allowed molecular desorption of various
The reverse water gas shift (RWGS) reaction catalyzed by barium zirconate-based perovskite-type catalysts doped with Y, Zn, and Ce was investigated in terms of activities and chemical stabilities of various catalysts. All of the catalysts showed stable performances for the RWGS reaction at 600 °C for 5 h, and in particular, the BaZr 0.8 Y 0.16 Zn 0.04 O 3 (BZYZ) catalyst showed an outstanding activity with an average CO 2 conversion of 37.5% and a CO selectivity of 97%. Insertion of additional C
Using a novel polymer (polythienothiophene-co-benzodithiophenes 7 F-20) as a donor and phenyl-C71-butyric acid methyl ester as an acceptor of bulk heterojunction, inverted organic photovoltaics (OPVs) were fabricated. Wet-chemically prepared ZnO and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) were used as buffer layers. Particularly, for PEDOT:PSS deposition, no annealing step was employed. This inverted OPV showed a power conversion efficiency (PCE) of ∼7.0%, which is co
We report a versatile and simple two-step method for fabricating superhydrophobic films with optical transparency. Silica nanoparticles were coated with a hydrophobic PDMS thin layer and subsequently fixed onto adhesive surfaces. The water contact angle on the prepared surface was over 150°, which implies that the surface is highly repellent to water. The transparent nature of the fabricated surface and its high chemical and physical stability were also demonstrated. Our method is simple, cost-e
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